510(k) K043408 ยท DZI Drill, Bone, Powered
PIEZOSURGERY DEVICE
| Applicant | Piezosurgery S.R.L., Rome, IT |
| Decision | Substantially Equivalent, Jun 8, 2005 |
| Received | Dec 10, 2004 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K043408
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.